Canonical Allele Identifier: CA2201699144
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1525975G= , CM000678.2:g.1525975G= GRCh38
NC_000016.9:g.1575976G= , CM000678.1:g.1575976G= GRCh37
NC_000016.8:g.1515977G= NCBI36
NG_032783.1:g.91134C=

Transcript Alleles

HGVS Amino-acid change
ENST00000426508.7:c.2680C= MANE Select ENSP00000406012.2:p.His894=
ENST00000361339.9:c.262C= ENSP00000354895.5:p.His88=
ENST00000397417.6:c.*1118C= ENSP00000380562.2:n.*1118C=
ENST00000426508.6:c.2680C= ENSP00000406012.2:p.His894=
ENST00000565298.5:n.1909C=
ENST00000566818.1:n.395C=
NM_014714.3:c.2680C= NP_055529.2:p.His894=
XM_006720989.2:c.2680C= XP_006721052.1:p.His894=
XM_006720990.2:c.2680C= XP_006721053.1:p.His894=
XM_006720991.2:c.2680C= XP_006721054.1:p.His894=
XM_006720992.2:c.313C= XP_006721055.1:p.His105=
XM_011522766.1:c.2434C= XP_011521068.1:p.His812=
XM_011522767.1:c.1705C= XP_011521069.1:p.His569=
XM_006720990.3:c.2680C= XP_006721053.1:p.His894=
XM_006720991.3:c.2680C= XP_006721054.1:p.His894=
XM_006720992.3:c.313C= XP_006721055.1:p.His105=
XM_011522766.3:c.2434C= XP_011521068.1:p.His812=
XM_011522767.2:c.1705C= XP_011521069.1:p.His569=
XM_017023910.1:c.2680C= XP_016879399.1:p.His894=
XM_017023911.1:c.865C= XP_016879400.1:p.His289=
NM_014714.4:c.2680C= MANE Select NP_055529.2:p.His894=